Canonical Allele Identifier: CA1546395361

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098607T= , CM000667.2:g.53098607T=	GRCh38
NC_000005.9:g.52394437T= , CM000667.1:g.52394437T=	GRCh37
NC_000005.8:g.52430194T=	NCBI36
NG_008435.2:g.16162A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.562A= MANE Select	ENSP00000380157.3:p.Ser188=
ENST00000450852.8:c.*482A= MANE Plus Clinical	ENSP00000411022.3:n.*482A=
ENST00000361377.8:c.*331A=	ENSP00000355160.4:n.*331A=
ENST00000396954.7:c.562A=	ENSP00000380157.3:p.Ser188=
ENST00000450852.7:c.*482A=	ENSP00000411022.3:n.*482A=
ENST00000502402.5:n.2309A=
ENST00000508922.5:c.*402A=	ENSP00000426274.1:n.*402A=
ENST00000510818.6:c.*435A=	ENSP00000424267.2:n.*435A=
ENST00000582677.5:c.*203A=	ENSP00000462870.1:n.*203A=
ENST00000584946.5:c.*354A=	ENSP00000464663.1:n.*354A=
NM_004531.4:c.562A=	NP_004522.1:p.Ser188=
NM_176806.3:c.*482A=	NP_789776.1:n.*482A=
NM_004531.5:c.562A= MANE Select	NP_004522.1:p.Ser188=
NM_176806.4:c.*482A= MANE Plus Clinical	NP_789776.1:n.*482A=